S 2101

S2101是一个赖氨酸特异性去甲基化酶1(LSD1)抑制剂，其IC50值为0.99μM，Ki值为0.61μM，Kinact/Ki值为4560M/s。

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库存: 现货

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5mg

￥2400.00

1920.00

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10mg

￥3775.00

3020.00

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25mg

￥7550.00

6040.00

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Background

S 2101 is a lysine-specific demethylase 1 (LSD1) inhibitor with an IC50 of 0.99 μM, Ki of 0.61 μM and Kinact/Ki of 4560 M/s.

S 2101 is a lysine-specific demethylase 1 (LSD1) inhibitor with an IC50 of 0.99 μM, Ki of 0.61 μM and Kinact/Ki of 4560 M/s. S 2101 also displays much lower inhibition activity toward MAO-B (Ki=17 µM, Kinact/Ki=18 M/s) and MAO-A (Ki=110 µM, Kinact/Ki=60 M/s). The treatment of HEK293T cells with S 2101 results in a dose-dependent increase in the level of H3K4me2, which must have accumulated by the inactivation of LSD1. During the course of S 2101 treatment, the amounts of histone H3 and LSD1 in the nuclear extracts remain essentially unaffected. Because the treatment with 1 μM S 2101 generates a level of H3K4me2 similar to that elicited by 50 μM 2-PCPA, S 2101 is assumed to have approximately 50-fold stronger LSD1 inhibition activity than 2-PCPA in human cells[1].

[1]. Mimasu S, et al. Structurally designed trans-2-phenylcyclopropylamine derivatives potently inhibit histone demethylase LSD1/KDM1 . Biochemistry. 2010 Aug 3;49(30):6494-503.

Protocol

Kinase experiment:

HEK293T cells are grown in 100 mm dishes in Dulbecco’s modified Eagle’s medium containing 10% FBS and a 100 units/mL penicillin, 100 μg/mL streptomycin antibiotic solution under a 5% CO2 atmosphere at 37°C. Cells at approximately 70% confluency are treated with S 2101 for 24 h, detached, and rinsed several times with ice-cold PBS. Nuclear extracts are prepared using a extraction kit, according to the manufacturer’s instructions. Each nuclear extract is electrophoresed on a 10 to 20% SDS-polyacrylamide gel and then transferred to a nitrocellulose membrane. The proteins on the membranes are probed with primary antibodies and then with a secondary antibody and are detected with a chemiluminescent system. The band intensities are visualized with an image analyzer[1].

参考文献:

[1]. Mimasu S, et al. Structurally designed trans-2-phenylcyclopropylamine derivatives potently inhibit histone demethylase LSD1/KDM1 . Biochemistry. 2010 Aug 3;49(30):6494-503.